Organopolysilozane compositions crosslinkable with elimination of alcohols to give elastomer
a technology of organic polysilozane and composition, which is applied in the field of alkoxy rtv1 composition, can solve the problems of compromising the consistency of the rtv-1 system, unsatisfactory stress-strain behavior of compositions used as permanently flexible sealing materials, and marked increase the danger of adhesion failure. , to achieve the effect of low modulus and convenient us
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example 1 (
inventive)
850 g of a dimethylpolysiloxane which has a hydroxyl group in each terminal unit and has a viscosity of 20,000 mPa.multidot.s at 23.degree. C. are mixed, in a planetary mixer which can operate under vacuum, with 12 g of a mixture of alkoxylated phosphoric esters of the formulae
(OH).sub.1 PO[(OCH.sub.2 CH.sub.2).sub.2-3 --O--(CH.sub.2).sub.7-9 --CH.sub.3 ].sub.2 and
(OH).sub.2 PO[(OCH.sub.2 CH.sub.2).sub.2-3 --O--(CH.sub.2).sub.7-9 --CH.sub.3 ].sub.1.
20 g of methyltrimethoxysilane, 10 g of vinyltrimethoxysilane and 10 g of dimethyldimethoxysilane are then immediately added, followed by homogenization at room temperature under normal pressure for 10 minutes. The following are then added in the sequence given, using the mixing techniques usual for RTV-1 compositions:
85 g of pyrogenic, hydrophilic silica with a BET surface area of 150 m.sup.2 / g, 18 g of amino-functional siloxane which is the equilibration product made from aminopropyltriethoxysilane and a condensate / hydrolysat...
example 2 (
inventive)
The procedure is similar to that of Example 1. 850 g of the .alpha.,.omega.-dihydroxypolydimethylsiloxane of Example 1 are mixed with 15 g of a mixture of alkoxylated phosphoric esters of the formulae
(OH).sub.1 PO[(OCH.sub.2 CH.sub.2).sub.3-4 --O--(CH.sub.2).sub.11-14--CH.sub.3 ].sub.2 and
(OH).sub.2 PO[(OCH.sub.2 CH.sub.2).sub.3-4 --O--(CH.sub.2).sub.11-14--CH.sub.3 ].sub.1.
To this the following ingredients are added in the sequence given:
22 g of methyltrimethoxysilane, 11 g of vinyltrimethoxysilane, 17 g of dimethyldimethoxysilane, 18 g of amino-functional siloxane which is the equilibration product made from aminopropyltriethoxysilane and a condensate / hydrolysate of methyltriethoxysilane with an amine number of 2.2, 4 g of 3-(2-aminoethylamino)propyltriethoxysilane, 85 g of pyrogenic, hydrophilic silica with a BET surface area of 150 m.sup.2 / g, and 4 g of the reaction product of tetraethyl silicate and di-n-butyltin diacetate from Example 1.
The skin-formation time of th...
example 3
The procedure is similar to that of Example 1. The following ingredients are admixed in the sequence given, employing 850 g of the .alpha.,.omega.-dihydroxypolydimethylsiloxane of Example 1: 15 g of the alkoxylated phosphoric ester of Example 2, 17 g of methyltrimethoxysilane, 8 g of vinyltrimethoxysilane and 25 g of dimethyldimethoxysilane are then added immediately, followed by homogenization in vacuo for 10 minutes. The following are then added in the sequence given, using the mixing techniques usual for RTV-1 compositions: 18 g of amino-functional siloxane which is the equilibration product made from aminopropyltriethoxysilane and a condensate / hydrolysate of methyltriethoxysilane with an amine number of 2.2, 4 g of 3-(2-aminoethylamino)propyltriethoxysilane, 85 g of pyrogenic, hydrophilic silica with a BET surface area of 150 m.sup.2 / g, and 4 g of the reaction product of tetraethyl silicate and di-n-butyltin diacetate from Example 1.
The skin-formation time of the composition du...
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